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1379001-47-4

C20H24N2O11 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379001-47-4 Structure

  • Basic information

    1. Product Name: C20H24N2O11
    2. Synonyms: C20H24N2O11
    3. CAS NO:1379001-47-4
    4. Molecular Formula:
    5. Molecular Weight: 468.417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379001-47-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C20H24N2O11(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H24N2O11(1379001-47-4)
    11. EPA Substance Registry System: C20H24N2O11(1379001-47-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1379001-47-4(Hazardous Substances Data)

1379001-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379001-47-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,0,0 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1379001-47:
(9*1)+(8*3)+(7*7)+(6*9)+(5*0)+(4*0)+(3*1)+(2*4)+(1*7)=154
154 % 10 = 4
So 1379001-47-4 is a valid CAS Registry Number.

1379001-47-4Relevant articles and documents

Facile synthesis of nitrophenyl 2-acetamido-2-deoxy-α-D- mannopyranosides from ManNAc-oxazoline

Krenek, Karel,Simon, Petr,Weignerova, Lenka,Fliedrova, Barbora,Kuzma, Marek,Kren, Vladimir

, p. 428 - 432 (2012/05/05)

The synthetic procedures for a large-scale preparation of o- and p-nitrophenyl 2-acetamido-2-deoxy-α-D-mannopyranoside are described. The synthetic pathway employs the glycosylation of phenol with ManNAc oxazoline, followed by nitration of the aromatic moiety yielding a separable mixture of the o- and p-nitrophenyl derivative in a 2:3 ratio.

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